Identification | More | [Name]
N-Carbobenzyloxy-L-glutamine | [CAS]
2650-64-8 | [Synonyms]
BENZYLOXYCARBONYL-L-GLUTAMINE CARBOBENZYLOXY-L-GLUTAMINE CBZ-GLN-OH CBZ-L-GLN CBZ-L-GLN-OH CBZ-L-GLUTAMINE N-ALPHA-BENZYLOXYCARBONYL-L-GLUTAMINE N-ALPHA-CARBOBENZOXY-L-GLUTAMINE NALPHA-CBZ-GLUTAMINE N(ALPHA)-CBZ-L-GLUTAMINE N-BENZYLOXYCARBONYL-L-GLUTAMINE N-CARBOBENZOXY-L-GLUTAMINE N-CARBOBENZYLOXY-L-GLUTAMINE N-CBZ-L-GLUTAMINE Z-GLN-OH Z-GLUTAMINE Z-L-GLN-OH Z-L-GLUTAMINE n2-[(phenylmethoxy)carbonyl]-l-glutamin N(alpha)-Benzyloxycarbonyl-L-glutamine~Z-Gln-OH | [EINECS(EC#)]
220-173-8 | [Molecular Formula]
C13H16N2O5 | [MDL Number]
MFCD00008043 | [Molecular Weight]
280.28 | [MOL File]
2650-64-8.mol |
Chemical Properties | Back Directory | [Appearance]
white to off-white powder | [Melting point ]
134-138 °C(lit.) | [alpha ]
-7 º (c=2, EtOH) | [Boiling point ]
423°C (rough estimate) | [density ]
1.2419 (rough estimate) | [refractive index ]
1.6450 (estimate) | [storage temp. ]
-20°C | [pka]
3.82±0.10(Predicted) | [optical activity]
[α]23/D 7.3°, c = 2 in ethanol | [BRN ]
2061271 | [InChIKey]
JIMLDJNLXLMGLX-JTQLQIEISA-N | [CAS DataBase Reference]
2650-64-8(CAS DataBase Reference) | [EPA Substance Registry System]
2650-64-8(EPA Substance) |
Safety Data | Back Directory | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [HazardClass ]
IRRITANT | [HS Code ]
29242990 |
Hazard Information | Back Directory | [Chemical Properties]
N-Carbobenzyloxy-L-glutamine is white to off-white powder
| [Uses]
N2-[(Phenylmethoxy)carbonyl]-L-glutamine has use an anti-ulcer agent. Also an inhibitor for AHAS (Acetohydroxy Acid Synthase) an important enzyme which will affect how benign an environmental herbicide is. Also used in the synthesis of neomycin B, an important HIV antiviral agent. | [Uses]
N-Carbobenzyloxy-L-glutamine has use an anti-ulcer agent. Also an inhibitor for AHAS (Acetohydroxy Acid Synthase) an important enzyme which will affect how benign an environmental herbicid e is. Also used in the synthesis of neomycin B, an important HIV antiviral agent.
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